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DSG1 Gene Erythroderma congenital with palmoplantar keratoderma hypotrichosis and hyper IgE Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The DSG1 Gene Erythroderma Congenital with Palmoplantar Keratoderma, Hypotrichosis, and Hyper IgE Genetic Test is a specialized diagnostic examination available at DNA Labs UAE. This test is designed to identify mutations in the DSG1 gene, which are linked to a rare genetic condition characterized by several dermatological and immunological symptoms. Individuals affected by this condition often exhibit erythroderma (redness and scaling of the skin), palmoplantar keratoderma (thickening of the skin on the palms and soles), hypotrichosis (reduced hair growth), and elevated levels of Immunoglobulin E (IgE), a type of antibody that plays a crucial role in the body’s immune response.

The test, priced at 4400 AED, involves collecting a DNA sample from the patient, typically through a blood draw or a cheek swab, and analyzing it for specific genetic alterations in the DSG1 gene. The results from this test can provide essential information for the diagnosis, management, and potential treatment of this complex condition. It is particularly valuable for affected individuals and their families for understanding the genetic basis of the disorder, informing clinical management, and genetic counseling. DNA Labs UAE is equipped with state-of-the-art technology and staffed by professionals with expertise in genetic testing, ensuring accurate and reliable results.

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DSG1 Gene Erythroderma congenital with palmoplantar keratoderma hypotrichosis and hyper IgE Genetic Test

Test Name: DSG1 Gene Erythroderma congenital with palmoplantar keratoderma hypotrichosis and hyper IgE Genetic Test

Components: DSG1 gene erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper IgE

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test type: Osteology Dermatology Immunology Disorders

Doctor: Dermatologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for DSG1 Gene Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis and hyper IgE NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DSG1 Gene Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis and hyper IgE NGS Genetic DNA Test gene DSG1

Test Details: DSG1 gene erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper IgE is a rare genetic disorder characterized by several symptoms. Erythroderma refers to a widespread redness and scaling of the skin, while palmoplantar keratoderma is a thickening of the skin on the palms and soles. Hypotrichosis refers to sparse or absent hair, and hyper IgE indicates elevated levels of immunoglobulin E, which is associated with allergic reactions.

NGS genetic testing, also known as next-generation sequencing, is a diagnostic tool used to analyze the DNA sequence of specific genes. In the case of DSG1 gene erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper IgE, NGS genetic testing can identify mutations or variations in the DSG1 gene that are responsible for causing the disorder. By identifying these genetic changes, NGS genetic testing can help confirm a diagnosis and provide valuable information for genetic counseling, treatment planning, and management of the condition. It can also be used for carrier testing and prenatal diagnosis in families with a known history of the disorder.

It’s important to note that while NGS genetic testing can provide valuable insights into the genetic basis of a condition, it may not be available in all healthcare settings and may not be covered by insurance. Additionally, the interpretation of genetic test results should always be done in consultation with a qualified healthcare professional or genetic counselor.

Test Name DSG1 Gene Erythroderma congenital with palmoplantar keratoderma hypotrichosis and hyper IgE Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for DSG1 Gene Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis and hyper IgE NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DSG1 Gene Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis and hyper IgE NGS Genetic DNA Test gene DSG1
Test Details

DSG1 gene erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper IgE is a rare genetic disorder characterized by several symptoms.

Erythroderma refers to a widespread redness and scaling of the skin, while palmoplantar keratoderma is a thickening of the skin on the palms and soles. Hypotrichosis refers to sparse or absent hair, and hyper IgE indicates elevated levels of immunoglobulin E, which is associated with allergic reactions.

NGS genetic testing, also known as next-generation sequencing, is a diagnostic tool used to analyze the DNA sequence of specific genes. In the case of DSG1 gene erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper IgE, NGS genetic testing can identify mutations or variations in the DSG1 gene that are responsible for causing the disorder.

By identifying these genetic changes, NGS genetic testing can help confirm a diagnosis and provide valuable information for genetic counseling, treatment planning, and management of the condition. It can also be used for carrier testing and prenatal diagnosis in families with a known history of the disorder.

It’s important to note that while NGS genetic testing can provide valuable insights into the genetic basis of a condition, it may not be available in all healthcare settings and may not be covered by insurance. Additionally, the interpretation of genetic test results should always be done in consultation with a qualified healthcare professional or genetic counselor.

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